Evidence map›Paper›PMID 30023299›Full record

ArticleMolecular genetics and metabolism reports2018

Genetic and clinical characteristics of Filipino patients with Gaucher disease.

Mary Anne D Chiong, Marie Julianne C Racoma, Mary Ann R Abacan

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular genetics and metabolism reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
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  3. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Mary Anne D ChiongInstitute of Human Genetics, National Institutes of Health University of the Philippines Manila, Philippines.
Marie Julianne C RacomaNewborn Screening Reference Center, National Institutes of Health, University of the Philippines, Manila, Philippines.
Mary Ann R AbacanInstitute of Human Genetics, National Institutes of Health University of the Philippines Manila, Philippines.
University of the Philippines Manila · PHUniversity of Santo Tomas · PH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gaucher disease (GD) is a lysosomal storage disorder caused by the deficiency of the β-glucocerebrosidase enzyme due to disease causing mutations in the

Indexed as

Enzyme replacement therapyFilipinosGaucher diseaseGBA1 mutationsSevere phenotypeβ glucocerebrosidase

Identifiers

PMID30023299
PMCPMC6047105
OpenAlexW2795979125

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.